R19T (p.Arg19Thr) variant of CDKN1B (P46527)
R19T (p.Arg19Thr) in CDKN1B (P46527) is a missense change. The record also includes structural context.
R19T (p.Arg19Thr) variant details
- p.Arg19Thr
- Ensembl rs1946487134
- Missense
- Structural context available